ClearanceBrief
510(k) K063653 ยท HCG Device, Neurovascular Embolization

MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC

ApplicantMicrus Endovascular Corporation, San Jose CA, US
DecisionSubstantially Equivalent, Jan 17, 2007
ReceivedDec 8, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K063653

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.